» Articles » PMID: 20376812

Separation of Dipeptides with Two Chiral Centers Using 2-hydroxypropyl-beta-CD-modified MEKC

Overview
Journal Electrophoresis
Specialty Chemistry
Date 2010 Apr 9
PMID 20376812
Citations 2
Authors
Affiliations
Soon will be listed here.
Abstract

A method was developed for the chiral separation of dipeptides with two chiral centers. Although all analyzed peptides contain chromophores and they can be detected by UV-adsorption detection without any derivatization, the chiral separations were not achieved for non-derivatized peptides using the same chiral selectors and experimental conditions. In this paper, these dipeptides were precolumn derivatized by using naphthalene-2, 3-dicarboxyaldehyde as a tagging reagent. In the presence of 2-hydroxypropyl-beta-CD and sodium deoxycholate, naphthalene-2,3-dicarboxyaldehyde-tagged dipeptide enantiomers were well resolved by MEKC. Good separation of all enantiomers was obtained within 14 min. The proposed method was applied to chiral separation of dipeptide enantiomers in spiked human serum samples.

Citing Articles

Bile Salts in Chiral Micellar Electrokinetic Chromatography: 2000-2020.

Yu R, Quirino J Molecules. 2021; 26(18).

PMID: 34577002 PMC: 8468585. DOI: 10.3390/molecules26185531.


In vitro evaluation of the protective effects of plant extracts against amyloid-beta peptide-induced toxicity in human neuroblastoma SH-SY5Y cells.

Sereia A, Oliveira M, Baranoski A, Marques L, Ribeiro F, Isolani R PLoS One. 2019; 14(2):e0212089.

PMID: 30763379 PMC: 6375598. DOI: 10.1371/journal.pone.0212089.